A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3951706



Internal ID21371776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:47179107..47179107hg38UCSC Ensembl
chr1:47644779..47644779hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15194218
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3951706
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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